Does anyone take topamax for MAV?
I am currently titrating up towards 100mg on topamax, i am on 65mg at moment and every time i increase the dose i always have worsening symptoms ie i become dizzier, more disequilibrium, more tingling hands and feet etc. I was just wondering if anyone else experiences the same? also is 100mg the max you can take for migraine or can you go higher? I can't really tell if it is helping me yet because i am always upping the dose and i have read on other forums that it can take a while to kick in any way. I would love to hear anybody elses experiences on this drug.